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Pazopanib-Induced Cutaneous Leukocytoclastic Vasculitis: An Exclusion Diagnosis of a Multidisciplinary Approach

dc.contributor.authorAlpuim Costa, D
dc.contributor.authorBaptista de Almeida, S
dc.contributor.authorCoelho Barata, P
dc.contributor.authorQuintela, A
dc.contributor.authorCabral, P
dc.contributor.authorAfonso, A
dc.contributor.authorMaia Silva, J
dc.date.accessioned2017-11-27T23:32:21Z
dc.date.available2017-11-27T23:32:21Z
dc.date.issued2017
dc.description.abstractIn phase II/III trials, cutaneous side effects of pazopanib were reported in less than 20% of patients, with only 1–3% being grade 3/4. We present a case of a 66-year-old man with a previous history of left nephrectomy for a stage II clear cell renal carcinoma. Approximately 18 months later, recurrent disease in the lungs, mediastinum, and left psoas and bulky abdominal/pelvic nodal metastasis were documented. He was initially treated with pazopanib 800 mg q.d. and 1 week after starting this therapy, the patient presented with palpable purpura on his ankles. These lesions regressed within 2 weeks off pazopanib, but had recurred 4 weeks after he resumed medication at 400 mg q.d. Biopsy of the lesions revealed leukocytoclastic vasculitis. Despite tumour response to therapy, pazopanib was discontinued with total resolution of this skin toxicity within 2 weeks of his cutaneous toxicity. To the best of our knowledge, we report a rare yet significant cutaneous adverse reaction to pazopanib.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationCase Rep Oncol 2017;10:1041-1049pt_PT
dc.identifier.doi10.1159/000484402pt_PT
dc.identifier.urihttp://hdl.handle.net/10400.26/19526
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.subjectVasculite Leucocitoclástica Cutânea/induzida quimicamentept_PT
dc.subjectPazopanib/efeitos adversospt_PT
dc.subjectVasculitis, Leukocytoclastic, Cutaneous/chemically inducedpt_PT
dc.subjectPazopanib/adverse effectspt_PT
dc.titlePazopanib-Induced Cutaneous Leukocytoclastic Vasculitis: An Exclusion Diagnosis of a Multidisciplinary Approachpt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage1049pt_PT
oaire.citation.startPage1041pt_PT
rcaap.rightsopenAccesspt_PT
rcaap.typearticlept_PT

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